Kim Min Jung, Son Hee Jin, Kim Yiseul, Kweon Hae-Jin, Suh Byung-Chang, Lyall Vijay, Rhyu Mee-Ra
Division of Metabolism and Functionality Research, Korea Food Research Institute, Bundang-gu, Sungnam-si, Gyeonggi-do, Republic of Korea.
Department of Brain Science, DaeguGyeongbuk Institute of Science and Technology (DGIST), Daegu, Republic of Korea.
PLoS One. 2014 Feb 20;9(2):e89062. doi: 10.1371/journal.pone.0089062. eCollection 2014.
TRPV1t, a variant of the transient receptor potential vanilloid-1 (TRPV1) has been proposed as a constitutively active, non-selective cation channel as a putative amiloride-insensitive salt taste receptor and shares many properties with TRPV1. Based on our previous chorda tympani taste nerve recordings in rodents and human sensory evaluations, we proposed that N-geranylcyclopropylcarboxamide (NGCC), a novel synthetic compound, acts as a salt taste enhancer by modulating the amiloride/benzamil-insensitive Na(+) entry pathways. As an extension of this work, we investigated NGCC-induced human TRPV1 (hTRPV1) activation using a Ca(2+)-flux signaling assay in cultured cells. NGCC enhanced Ca(2+) influx in hTRPV1-expressing cells in a dose-dependent manner (EC50 = 115 µM). NGCC-induced Ca(2+) influx was significantly attenuated by ruthenium red (RR; 30 µM), a non-specific blocker of TRP channels and capsazepine (CZP; 5 µM), a specific antagonist of TRPV1, implying that NGCC directly activates hTRPV1. TRPA1 is often co-expressed with TRPV1 in sensory neurons. Therefore, we also investigated the effects of NGCC on hTRPA1-expressing cells. Similar to hTRPV1, NGCC enhanced Ca(2+) influx in hTRPA1-expressing cells (EC50 = 83.65 µM). The NGCC-induced Ca(2+) influx in hTRPA1-expressing cells was blocked by RR (30 µM) and HC-030031 (100 µM), a specific antagonist of TRPA1. These results suggested that NGCC selectively activates TRPV1 and TRPA1 in cultured cells. These data may provide additional support for our previous hypothesis that NGCC interacts with TRPV1 variant cation channel, a putative amiloride/benzamil-insensitive salt taste pathway in the anterior taste receptive field.
瞬时受体电位香草酸受体1(TRPV1)的变体TRPV1t已被提出是一种组成型活性、非选择性阳离子通道,作为一种假定的amiloride不敏感盐味受体,与TRPV1具有许多共同特性。基于我们之前在啮齿动物中的鼓索味觉神经记录和人类感官评估,我们提出新型合成化合物N-香叶基环丙基甲酰胺(NGCC)通过调节amiloride/benzamil不敏感的Na(+)进入途径来充当盐味增强剂。作为这项工作的延伸,我们在培养细胞中使用Ca(2+)通量信号测定法研究了NGCC诱导的人类TRPV1(hTRPV1)激活。NGCC以剂量依赖性方式增强了表达hTRPV1的细胞中的Ca(2+)内流(EC50 = 115 µM)。TRP通道的非特异性阻滞剂钌红(RR;30 µM)和TRPV1的特异性拮抗剂辣椒素(CZP;5 µM)显著减弱了NGCC诱导的Ca(2+)内流,这意味着NGCC直接激活hTRPV1。TRPA1在感觉神经元中常与TRPV1共表达。因此,我们还研究了NGCC对表达hTRPA1的细胞的影响。与hTRPV1类似,NGCC增强了表达hTRPA1的细胞中的Ca(2+)内流(EC50 = 83.65 µM)。RR(30 µM)和TRPA1的特异性拮抗剂HC-030031(100 µM)阻断了NGCC诱导的表达hTRPA1的细胞中的Ca(2+)内流。这些结果表明NGCC在培养细胞中选择性激活TRPV1和TRPA1。这些数据可能为我们之前的假设提供额外支持,即NGCC与TRPV1变体阳离子通道相互作用,这是前味觉感受区域中一种假定的amiloride/benzamil不敏感盐味途径。